ODCs

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1 OMIM reference -
1 associated gene
19 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1

1 OMIM reference -
4 associated genes
14 signs/symptoms

Carnitine palmitoyl transferase 1A deficiency

Follicular lymphoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CPT1A	(0.67)	BCL2

Citations in the biomedical literature:

Carnitine palmitoyl transferase 1A deficiency		Follicular lymphoma
	Synonym(s): - CPT1A deficiency - Carnitine palmitoyl transferase IA deficiency - Hepatic carnitine palmitoyl transferase 1 deficiency - Hepatic carnitine palmitoyl transferase I deficiency - L-CPT1 deficiency - L-CPTI deficiency		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: adulthood Average age of death: adult Type of inheritance: multigenic/multifactorial

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D008224

Carnitine palmitoyl transferase 1A deficiency		Follicular lymphoma
	Very frequent - Areflexia / hyporeflexia - Autosomal recessive inheritance - Hepatocellular liver disease / hepatic failure - Hypoglycemia - Hypotonia - Metabolic anomalies - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Psychic / behavioural troubles - Seizures / epilepsy / absences / spasms / status epilepticus - Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia Frequent - Hemiplegia / diplegia / hemiparesia / limb palsy - Hepatomegaly / liver enlargement (excluding storage disease) - Hyperlipidemia / hypercholesterolemia / hypertriglyceridemia - Obnubilation / coma / lethargia / desorientation Occasional - Cardiac rhythm disorder / arrhythmia - Cardiomyopathy / hypertrophic / dilated - Collapse / sudden death / cardiac arrest / cardiorespiratory arrest - Renal tubular defect / tubulopathy		Very frequent - Fever / chilling - Hematologic / blood / lymphatic cancer - Hyperhidrosis / increased sweating - Lymphadenopathy / polyadenopathies - Weight loss / loss of appetite / break in weight curve / general health alteration Frequent - Mediastinal / hilar adenopathies - Splenomegaly Occasional - Abnormal pleura / hydrothorax / pleuresia / pleural effusion / chylothorax - Anomalies of skin, subcutaneous tissue and mucosae - Bone marrow / medullar infiltration - Lymphedema - Meningitis / meningeal syndrome - Structural anomaly of the peritoneum